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Tempered optimism: Advances in the precision medicine era for pediatric low-grade glioma
Chelsea Kotch1,2, Sebastien Perreault3, Phoebe Power4,5
1Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Abstract:
The clinical trial landscape of molecularly targeted treatments for pediatric low-grade glioma (pLGG) has created an exciting and hopeful era for both patients and clinicians alike. Despite numerous clinical trials investigating the use of targeted agents for pLGG, only two oral precision-based regimens for pLGG have received federal agency approval. However, enthusiasm surrounding recently completed early phase clinical trials has resulted in increased off-label prescribing practices beyond the federally-approved indications, despite a lack of phase 3 clinical trial data and an incomplete understanding of the long-term radiographic, functional outcomes, and toxicity for both approved and experimental therapies. These gaps in knowledge are critically important to consider when selecting therapies for patients with pLGG, as the prevention and reduction of late effects in pLGG survivors is crucial to prevent long-term morbidity. In this editorial by the clinical working group of the International pLGG Coalition, we discuss the landscape of molecularly targeted therapies for pLGG, outline the unanswered questions for the use of novel therapies in the management of pLGG, review the risks and benefits of early off-label use of targeted agents, and discuss the importance of patience and evidence-based clinical practice in the rapidly evolving era of precision medicine.
Insights
Molecularly targeted therapies offer hope for pediatric low-grade glioma (pLGG), but off-label use lacks phase 3 data. Evidence-based practice is crucial for managing pLGG and preventing long-term effects in survivors.
Area of Science:
- Pediatric Oncology
- Molecular Targeted Therapy
- Precision Medicine
Background:
- The treatment landscape for pediatric low-grade glioma (pLGG) is evolving with molecularly targeted therapies.
- Only two oral precision regimens are FDA-approved for pLGG, despite numerous clinical trials.
- Off-label prescribing of targeted agents is increasing, driven by early-phase trial enthusiasm.
Purpose of the Study:
- To discuss the current landscape of molecularly targeted therapies for pLGG.
- To outline unanswered questions regarding novel therapies in pLGG management.
- To review the risks and benefits of early off-label targeted agent use.
Main Methods:
- Editorial review of the clinical trial landscape for pLGG.
- Discussion of approved and experimental targeted therapies.
- Analysis of off-label prescribing practices and knowledge gaps.
Main Results:
- Limited federal approval for targeted pLGG therapies contrasts with increased off-label use.
- Significant gaps exist in phase 3 data for long-term outcomes and toxicity of targeted agents.
- The need for evidence-based clinical practice is highlighted.
Conclusions:
- Careful consideration of knowledge gaps is essential when selecting pLGG therapies.
- Preventing long-term morbidity in pLGG survivors requires understanding treatment effects.
- Patience and evidence-based approaches are vital in the era of precision medicine for pLGG.
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